Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism

The study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages’ phagocytosis ability in engulfi...

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Main Authors: Mohsen S. Al-Omar, Majid Jabir, Esraa Karsh, Rua Kadhim, Ghassan M. Sulaiman, Zainab J. Taqi, Khawla S. Khashan, Hamdoon A. Mohammed, Riaz A. Khan, Salman A. A. Mohammed
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/11/6/1382
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author Mohsen S. Al-Omar
Majid Jabir
Esraa Karsh
Rua Kadhim
Ghassan M. Sulaiman
Zainab J. Taqi
Khawla S. Khashan
Hamdoon A. Mohammed
Riaz A. Khan
Salman A. A. Mohammed
author_facet Mohsen S. Al-Omar
Majid Jabir
Esraa Karsh
Rua Kadhim
Ghassan M. Sulaiman
Zainab J. Taqi
Khawla S. Khashan
Hamdoon A. Mohammed
Riaz A. Khan
Salman A. A. Mohammed
author_sort Mohsen S. Al-Omar
collection DOAJ
description The study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages’ phagocytosis ability in engulfing, thereby annihilating the cancer cells in both in vitro and in vivo conditions. The GNPs and GOFs augmented serine protease class apoptotic protein, granzyme, passing through the aquaporin class protein, perforin, with mediated delivery through the cell membrane site for the programmed, calibrated, and conditioned cancer cells killing. Additionally, protease inhibitor 3,4-dichloroisocoumarin (DCI) significantly reduced granzyme and perforin activities of macrophages. The results demonstrated that the GOFs and GNPs increased the activation of phagocytic cells as a promising strategy for controlling cancer cells by augmenting the cell mortality through the granzyme-perforin-dependent mechanism.
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spelling doaj.art-a77be7dec2f54ce9b5ba0f39b089a88d2023-11-21T21:06:42ZengMDPI AGNanomaterials2079-49912021-05-01116138210.3390/nano11061382Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent BiomechanismMohsen S. Al-Omar0Majid Jabir1Esraa Karsh2Rua Kadhim3Ghassan M. Sulaiman4Zainab J. Taqi5Khawla S. Khashan6Hamdoon A. Mohammed7Riaz A. Khan8Salman A. A. Mohammed9Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Qassim 51452, Saudi ArabiaDepartment of Applied Sciences, University of Technology, Baghdad 10066, IraqDepartment of Applied Sciences, University of Technology, Baghdad 10066, IraqDepartment of Applied Sciences, University of Technology, Baghdad 10066, IraqDepartment of Applied Sciences, University of Technology, Baghdad 10066, IraqDepartment of Applied Sciences, University of Technology, Baghdad 10066, IraqDepartment of Applied Sciences, University of Technology, Baghdad 10066, IraqDepartment of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Qassim 51452, Saudi ArabiaDepartment of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Qassim 51452, Saudi ArabiaDepartment of Pharmacology and Toxicology, College of Pharmacy, Qassim University, Qassim 51452, Saudi ArabiaThe study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages’ phagocytosis ability in engulfing, thereby annihilating the cancer cells in both in vitro and in vivo conditions. The GNPs and GOFs augmented serine protease class apoptotic protein, granzyme, passing through the aquaporin class protein, perforin, with mediated delivery through the cell membrane site for the programmed, calibrated, and conditioned cancer cells killing. Additionally, protease inhibitor 3,4-dichloroisocoumarin (DCI) significantly reduced granzyme and perforin activities of macrophages. The results demonstrated that the GOFs and GNPs increased the activation of phagocytic cells as a promising strategy for controlling cancer cells by augmenting the cell mortality through the granzyme-perforin-dependent mechanism.https://www.mdpi.com/2079-4991/11/6/1382graphene oxide flakesGOFsgold nanoparticlesGNPsphagocytosisSKOV-3
spellingShingle Mohsen S. Al-Omar
Majid Jabir
Esraa Karsh
Rua Kadhim
Ghassan M. Sulaiman
Zainab J. Taqi
Khawla S. Khashan
Hamdoon A. Mohammed
Riaz A. Khan
Salman A. A. Mohammed
Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism
Nanomaterials
graphene oxide flakes
GOFs
gold nanoparticles
GNPs
phagocytosis
SKOV-3
title Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism
title_full Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism
title_fullStr Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism
title_full_unstemmed Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism
title_short Gold Nanoparticles and Graphene Oxide Flakes Enhance Cancer Cells’ Phagocytosis through Granzyme-Perforin-Dependent Biomechanism
title_sort gold nanoparticles and graphene oxide flakes enhance cancer cells phagocytosis through granzyme perforin dependent biomechanism
topic graphene oxide flakes
GOFs
gold nanoparticles
GNPs
phagocytosis
SKOV-3
url https://www.mdpi.com/2079-4991/11/6/1382
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